EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID20234022

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID20234022


InChI Key	PIJCMXDNWDLQTC-CLJLJLNGSA-N
Smiles	CC(CCc1ccccc1)N(CC(=O)c1cc(C(=O)N)c(OCc2ccccc2)cc1)C(C)c1ccccc1
InChI	InChI=1S/C34H36N2O3/c1-25(18-19-27-12-6-3-7-13-27)36(26(2)29-16-10-5-11-17-29)23-32(37)30-20-21-33(31(22-30)34(35)38)39-24-28-14-8-4-9-15-28/h3-17,20-22,25-26H,18-19,23-24H2,1-2H3,(H2,35,38)/t25-,26-/m0/s1

InChI Key

PIJCMXDNWDLQTC-CLJLJLNGSA-N

Smiles

CC(CCc1ccccc1)N(CC(=O)c1cc(C(=O)N)c(OCc2ccccc2)cc1)C(C)c1ccccc1

InChI

InChI=1S/C34H36N2O3/c1-25(18-19-27-12-6-3-7-13-27)36(26(2)29-16-10-5-11-17-29)23-32(37)30-20-21-33(31(22-30)34(35)38)39-24-28-14-8-4-9-15-28/h3-17,20-22,25-26H,18-19,23-24H2,1-2H3,(H2,35,38)/t25-,26-/m0/s1

Property Name	Value
Molecular Formula	C34H36N2O3
Molecular Weight	520.27
AlogP	7.42
Hydrogen Bond Acceptor	4.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	13.0
Polar Surface Area	73.62
Heavy Atoms	39.0

Property Name

Value

Molecular Formula

C34H36N2O3

Molecular Weight

520.27

AlogP

7.42

Hydrogen Bond Acceptor

4.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

13.0

Polar Surface Area

73.62

Heavy Atoms

39.0

Resources	Reference
CAS NUMBER	84963-37-1
NORMAN SUSDAT
PubChem	14097325
ChemSpider	34998992.0

Resources

Reference

CAS NUMBER

84963-37-1

NORMAN SUSDAT

PubChem

14097325

ChemSpider

34998992.0

EcoDrug+ was developed under the PREMIER Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information EcoDrug+ contains.

Elements of EcoDrug+ were developed under the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT Center for Science Ltd is thanked for providing computational resources. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

Content of EcoDrug+ is provided without guarantee for correctness.

Cite Us:

Ashenafi Legehar, Siobhán Monaghan, Mael Briand, Akseli Niemelä, Leo Ghemtio, Ziaurrehman Tanoli, A Ross Brown, Charles R Tyler, Henri Xhaard, EcoDrug PLUS: an advanced database for drug target conservation analysis and environmental risk assessment, Nucleic Acids Research, 2025, gkaf1251 Read...

This work is licensed under Creative Commons Attribution-ShareAlike 4.0 International License

Last update: Monday, 3 November 2025

(R-(R,R))-2-(BENZYLOXY)-5-(((1-METHYL-3-PHENYLPROPYL)(1-PHENYLETHYL)AMINO)ACETYL)BENZAMIDE

Structure

Physicochemical Descriptors

Cross References

(R-(R*,R*))-2-(BENZYLOXY)-5-(((1-METHYL-3-PHENYLPROPYL)(1-PHENYLETHYL)AMINO)ACETYL)BENZAMIDE

Structure

Physicochemical Descriptors

Cross References

(R-(R,R))-2-(BENZYLOXY)-5-(((1-METHYL-3-PHENYLPROPYL)(1-PHENYLETHYL)AMINO)ACETYL)BENZAMIDE